Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries
Abstract Iron disulfide ($ FeS_{2} $) powders were successfully synthesized by hydrothermal method. Cetyltrimethylammonium bromide (CTAB) had a great influence on the morphology, particle size, and electrochemical performance of the $ FeS_{2} $ powders. The as-synthesized $ FeS_{2} $ particles with...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Zhang, D. [verfasserIn] Wang, X. L. [verfasserIn] Mai, Y. J. [verfasserIn] Xia, X. H. [verfasserIn] Gu, C. D. [verfasserIn] Tu, J. P. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2012 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Journal of applied electrochemistry - Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971, 42(2012), 4 vom: 24. Feb., Seite 263-269 |
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| Übergeordnetes Werk: |
volume:42 ; year:2012 ; number:4 ; day:24 ; month:02 ; pages:263-269 |
| Links: |
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| DOI / URN: |
10.1007/s10800-012-0393-5 |
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| Katalog-ID: |
SPR013309722 |
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| 245 | 1 | 0 | |a Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries |
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| 520 | |a Abstract Iron disulfide ($ FeS_{2} $) powders were successfully synthesized by hydrothermal method. Cetyltrimethylammonium bromide (CTAB) had a great influence on the morphology, particle size, and electrochemical performance of the $ FeS_{2} $ powders. The as-synthesized $ FeS_{2} $ particles with CTAB had diameters of 2–4 μm and showed a sphere-like structure with sawtooth, while the counterpart prepared without CTAB exhibited irregular morphology with diameters in the range of 0.1–0.4 μm. As anode materials for Li-ion batteries, their electrochemical performances were investigated by galvanostatic charge–discharge test and electrochemical impedance spectrum. The $ FeS_{2} $ powder synthesized with CTAB can sustain 459 and 413 mAh $ g^{−1} $ at 89 and 445 mA $ g^{−1} $ after 35 cycles, respectively, much higher than those prepared without CTAB (411 and 316 mAh $ g^{−1} $). The enhanced rate capability and cycling stability were attributed to the less-hindered surface layer and better electrical contact from the sawtooth-like surface and micro-sized sphere morphology, which led to enhanced process kinetics. | ||
| 650 | 4 | |a Iron disulfide |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Marcasite |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Rate capability |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Cycling performance |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Wang, X. L. |e verfasserin |4 aut | |
| 700 | 1 | |a Mai, Y. J. |e verfasserin |4 aut | |
| 700 | 1 | |a Xia, X. H. |e verfasserin |4 aut | |
| 700 | 1 | |a Gu, C. D. |e verfasserin |4 aut | |
| 700 | 1 | |a Tu, J. P. |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Journal of applied electrochemistry |d Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971 |g 42(2012), 4 vom: 24. Feb., Seite 263-269 |w (DE-627)302466037 |w (DE-600)1491094-9 |x 1572-8838 |7 nnns |
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2012 |
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10.1007/s10800-012-0393-5 doi (DE-627)SPR013309722 (SPR)s10800-012-0393-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl Zhang, D. verfasserin aut Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Iron disulfide ($ FeS_{2} $) powders were successfully synthesized by hydrothermal method. Cetyltrimethylammonium bromide (CTAB) had a great influence on the morphology, particle size, and electrochemical performance of the $ FeS_{2} $ powders. The as-synthesized $ FeS_{2} $ particles with CTAB had diameters of 2–4 μm and showed a sphere-like structure with sawtooth, while the counterpart prepared without CTAB exhibited irregular morphology with diameters in the range of 0.1–0.4 μm. As anode materials for Li-ion batteries, their electrochemical performances were investigated by galvanostatic charge–discharge test and electrochemical impedance spectrum. The $ FeS_{2} $ powder synthesized with CTAB can sustain 459 and 413 mAh $ g^{−1} $ at 89 and 445 mA $ g^{−1} $ after 35 cycles, respectively, much higher than those prepared without CTAB (411 and 316 mAh $ g^{−1} $). The enhanced rate capability and cycling stability were attributed to the less-hindered surface layer and better electrical contact from the sawtooth-like surface and micro-sized sphere morphology, which led to enhanced process kinetics. Iron disulfide (dpeaa)DE-He213 Marcasite (dpeaa)DE-He213 Rate capability (dpeaa)DE-He213 Cycling performance (dpeaa)DE-He213 Wang, X. L. verfasserin aut Mai, Y. J. verfasserin aut Xia, X. H. verfasserin aut Gu, C. D. verfasserin aut Tu, J. P. verfasserin aut Enthalten in Journal of applied electrochemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971 42(2012), 4 vom: 24. Feb., Seite 263-269 (DE-627)302466037 (DE-600)1491094-9 1572-8838 nnns volume:42 year:2012 number:4 day:24 month:02 pages:263-269 https://dx.doi.org/10.1007/s10800-012-0393-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE AR 42 2012 4 24 02 263-269 |
| spelling |
10.1007/s10800-012-0393-5 doi (DE-627)SPR013309722 (SPR)s10800-012-0393-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl Zhang, D. verfasserin aut Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Iron disulfide ($ FeS_{2} $) powders were successfully synthesized by hydrothermal method. Cetyltrimethylammonium bromide (CTAB) had a great influence on the morphology, particle size, and electrochemical performance of the $ FeS_{2} $ powders. The as-synthesized $ FeS_{2} $ particles with CTAB had diameters of 2–4 μm and showed a sphere-like structure with sawtooth, while the counterpart prepared without CTAB exhibited irregular morphology with diameters in the range of 0.1–0.4 μm. As anode materials for Li-ion batteries, their electrochemical performances were investigated by galvanostatic charge–discharge test and electrochemical impedance spectrum. The $ FeS_{2} $ powder synthesized with CTAB can sustain 459 and 413 mAh $ g^{−1} $ at 89 and 445 mA $ g^{−1} $ after 35 cycles, respectively, much higher than those prepared without CTAB (411 and 316 mAh $ g^{−1} $). The enhanced rate capability and cycling stability were attributed to the less-hindered surface layer and better electrical contact from the sawtooth-like surface and micro-sized sphere morphology, which led to enhanced process kinetics. Iron disulfide (dpeaa)DE-He213 Marcasite (dpeaa)DE-He213 Rate capability (dpeaa)DE-He213 Cycling performance (dpeaa)DE-He213 Wang, X. L. verfasserin aut Mai, Y. J. verfasserin aut Xia, X. H. verfasserin aut Gu, C. D. verfasserin aut Tu, J. P. verfasserin aut Enthalten in Journal of applied electrochemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971 42(2012), 4 vom: 24. Feb., Seite 263-269 (DE-627)302466037 (DE-600)1491094-9 1572-8838 nnns volume:42 year:2012 number:4 day:24 month:02 pages:263-269 https://dx.doi.org/10.1007/s10800-012-0393-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE AR 42 2012 4 24 02 263-269 |
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10.1007/s10800-012-0393-5 doi (DE-627)SPR013309722 (SPR)s10800-012-0393-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl Zhang, D. verfasserin aut Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Iron disulfide ($ FeS_{2} $) powders were successfully synthesized by hydrothermal method. Cetyltrimethylammonium bromide (CTAB) had a great influence on the morphology, particle size, and electrochemical performance of the $ FeS_{2} $ powders. The as-synthesized $ FeS_{2} $ particles with CTAB had diameters of 2–4 μm and showed a sphere-like structure with sawtooth, while the counterpart prepared without CTAB exhibited irregular morphology with diameters in the range of 0.1–0.4 μm. As anode materials for Li-ion batteries, their electrochemical performances were investigated by galvanostatic charge–discharge test and electrochemical impedance spectrum. The $ FeS_{2} $ powder synthesized with CTAB can sustain 459 and 413 mAh $ g^{−1} $ at 89 and 445 mA $ g^{−1} $ after 35 cycles, respectively, much higher than those prepared without CTAB (411 and 316 mAh $ g^{−1} $). The enhanced rate capability and cycling stability were attributed to the less-hindered surface layer and better electrical contact from the sawtooth-like surface and micro-sized sphere morphology, which led to enhanced process kinetics. Iron disulfide (dpeaa)DE-He213 Marcasite (dpeaa)DE-He213 Rate capability (dpeaa)DE-He213 Cycling performance (dpeaa)DE-He213 Wang, X. L. verfasserin aut Mai, Y. J. verfasserin aut Xia, X. H. verfasserin aut Gu, C. D. verfasserin aut Tu, J. P. verfasserin aut Enthalten in Journal of applied electrochemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971 42(2012), 4 vom: 24. Feb., Seite 263-269 (DE-627)302466037 (DE-600)1491094-9 1572-8838 nnns volume:42 year:2012 number:4 day:24 month:02 pages:263-269 https://dx.doi.org/10.1007/s10800-012-0393-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE AR 42 2012 4 24 02 263-269 |
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10.1007/s10800-012-0393-5 doi (DE-627)SPR013309722 (SPR)s10800-012-0393-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl Zhang, D. verfasserin aut Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Iron disulfide ($ FeS_{2} $) powders were successfully synthesized by hydrothermal method. Cetyltrimethylammonium bromide (CTAB) had a great influence on the morphology, particle size, and electrochemical performance of the $ FeS_{2} $ powders. The as-synthesized $ FeS_{2} $ particles with CTAB had diameters of 2–4 μm and showed a sphere-like structure with sawtooth, while the counterpart prepared without CTAB exhibited irregular morphology with diameters in the range of 0.1–0.4 μm. As anode materials for Li-ion batteries, their electrochemical performances were investigated by galvanostatic charge–discharge test and electrochemical impedance spectrum. The $ FeS_{2} $ powder synthesized with CTAB can sustain 459 and 413 mAh $ g^{−1} $ at 89 and 445 mA $ g^{−1} $ after 35 cycles, respectively, much higher than those prepared without CTAB (411 and 316 mAh $ g^{−1} $). The enhanced rate capability and cycling stability were attributed to the less-hindered surface layer and better electrical contact from the sawtooth-like surface and micro-sized sphere morphology, which led to enhanced process kinetics. Iron disulfide (dpeaa)DE-He213 Marcasite (dpeaa)DE-He213 Rate capability (dpeaa)DE-He213 Cycling performance (dpeaa)DE-He213 Wang, X. L. verfasserin aut Mai, Y. J. verfasserin aut Xia, X. H. verfasserin aut Gu, C. D. verfasserin aut Tu, J. P. verfasserin aut Enthalten in Journal of applied electrochemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971 42(2012), 4 vom: 24. Feb., Seite 263-269 (DE-627)302466037 (DE-600)1491094-9 1572-8838 nnns volume:42 year:2012 number:4 day:24 month:02 pages:263-269 https://dx.doi.org/10.1007/s10800-012-0393-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE AR 42 2012 4 24 02 263-269 |
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10.1007/s10800-012-0393-5 doi (DE-627)SPR013309722 (SPR)s10800-012-0393-5-e DE-627 ger DE-627 rakwb eng 540 ASE 35.14 bkl Zhang, D. verfasserin aut Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Iron disulfide ($ FeS_{2} $) powders were successfully synthesized by hydrothermal method. Cetyltrimethylammonium bromide (CTAB) had a great influence on the morphology, particle size, and electrochemical performance of the $ FeS_{2} $ powders. The as-synthesized $ FeS_{2} $ particles with CTAB had diameters of 2–4 μm and showed a sphere-like structure with sawtooth, while the counterpart prepared without CTAB exhibited irregular morphology with diameters in the range of 0.1–0.4 μm. As anode materials for Li-ion batteries, their electrochemical performances were investigated by galvanostatic charge–discharge test and electrochemical impedance spectrum. The $ FeS_{2} $ powder synthesized with CTAB can sustain 459 and 413 mAh $ g^{−1} $ at 89 and 445 mA $ g^{−1} $ after 35 cycles, respectively, much higher than those prepared without CTAB (411 and 316 mAh $ g^{−1} $). The enhanced rate capability and cycling stability were attributed to the less-hindered surface layer and better electrical contact from the sawtooth-like surface and micro-sized sphere morphology, which led to enhanced process kinetics. Iron disulfide (dpeaa)DE-He213 Marcasite (dpeaa)DE-He213 Rate capability (dpeaa)DE-He213 Cycling performance (dpeaa)DE-He213 Wang, X. L. verfasserin aut Mai, Y. J. verfasserin aut Xia, X. H. verfasserin aut Gu, C. D. verfasserin aut Tu, J. P. verfasserin aut Enthalten in Journal of applied electrochemistry Dordrecht [u.a.] : Springer Science + Business Media B.V, 1971 42(2012), 4 vom: 24. Feb., Seite 263-269 (DE-627)302466037 (DE-600)1491094-9 1572-8838 nnns volume:42 year:2012 number:4 day:24 month:02 pages:263-269 https://dx.doi.org/10.1007/s10800-012-0393-5 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.14 ASE AR 42 2012 4 24 02 263-269 |
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Enthalten in Journal of applied electrochemistry 42(2012), 4 vom: 24. Feb., Seite 263-269 volume:42 year:2012 number:4 day:24 month:02 pages:263-269 |
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Enthalten in Journal of applied electrochemistry 42(2012), 4 vom: 24. Feb., Seite 263-269 volume:42 year:2012 number:4 day:24 month:02 pages:263-269 |
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Iron disulfide Marcasite Rate capability Cycling performance |
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Journal of applied electrochemistry |
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Zhang, D. @@aut@@ Wang, X. L. @@aut@@ Mai, Y. J. @@aut@@ Xia, X. H. @@aut@@ Gu, C. D. @@aut@@ Tu, J. P. @@aut@@ |
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<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">SPR013309722</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230519082624.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">201006s2012 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s10800-012-0393-5</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)SPR013309722</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(SPR)s10800-012-0393-5-e</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">540</subfield><subfield code="q">ASE</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">35.14</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Zhang, D.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2012</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Iron disulfide ($ FeS_{2} $) powders were successfully synthesized by hydrothermal method. Cetyltrimethylammonium bromide (CTAB) had a great influence on the morphology, particle size, and electrochemical performance of the $ FeS_{2} $ powders. The as-synthesized $ FeS_{2} $ particles with CTAB had diameters of 2–4 μm and showed a sphere-like structure with sawtooth, while the counterpart prepared without CTAB exhibited irregular morphology with diameters in the range of 0.1–0.4 μm. As anode materials for Li-ion batteries, their electrochemical performances were investigated by galvanostatic charge–discharge test and electrochemical impedance spectrum. The $ FeS_{2} $ powder synthesized with CTAB can sustain 459 and 413 mAh $ g^{−1} $ at 89 and 445 mA $ g^{−1} $ after 35 cycles, respectively, much higher than those prepared without CTAB (411 and 316 mAh $ g^{−1} $). The enhanced rate capability and cycling stability were attributed to the less-hindered surface layer and better electrical contact from the sawtooth-like surface and micro-sized sphere morphology, which led to enhanced process kinetics.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Iron disulfide</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Marcasite</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Rate capability</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Cycling performance</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Wang, X. 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Zhang, D. |
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Zhang, D. ddc 540 bkl 35.14 misc Iron disulfide misc Marcasite misc Rate capability misc Cycling performance Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries |
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540 ASE 35.14 bkl Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries Iron disulfide (dpeaa)DE-He213 Marcasite (dpeaa)DE-He213 Rate capability (dpeaa)DE-He213 Cycling performance (dpeaa)DE-He213 |
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ddc 540 bkl 35.14 misc Iron disulfide misc Marcasite misc Rate capability misc Cycling performance |
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ddc 540 bkl 35.14 misc Iron disulfide misc Marcasite misc Rate capability misc Cycling performance |
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ddc 540 bkl 35.14 misc Iron disulfide misc Marcasite misc Rate capability misc Cycling performance |
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Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries |
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Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries |
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Zhang, D. |
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Journal of applied electrochemistry |
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Zhang, D. Wang, X. L. Mai, Y. J. Xia, X. H. Gu, C. D. Tu, J. P. |
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540 ASE 35.14 bkl |
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Elektronische Aufsätze |
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Zhang, D. |
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10.1007/s10800-012-0393-5 |
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verfasserin |
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enhanced electrochemical performance of $ fes_{2} $ synthesized by hydrothermal method for lithium ion batteries |
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Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries |
| abstract |
Abstract Iron disulfide ($ FeS_{2} $) powders were successfully synthesized by hydrothermal method. Cetyltrimethylammonium bromide (CTAB) had a great influence on the morphology, particle size, and electrochemical performance of the $ FeS_{2} $ powders. The as-synthesized $ FeS_{2} $ particles with CTAB had diameters of 2–4 μm and showed a sphere-like structure with sawtooth, while the counterpart prepared without CTAB exhibited irregular morphology with diameters in the range of 0.1–0.4 μm. As anode materials for Li-ion batteries, their electrochemical performances were investigated by galvanostatic charge–discharge test and electrochemical impedance spectrum. The $ FeS_{2} $ powder synthesized with CTAB can sustain 459 and 413 mAh $ g^{−1} $ at 89 and 445 mA $ g^{−1} $ after 35 cycles, respectively, much higher than those prepared without CTAB (411 and 316 mAh $ g^{−1} $). The enhanced rate capability and cycling stability were attributed to the less-hindered surface layer and better electrical contact from the sawtooth-like surface and micro-sized sphere morphology, which led to enhanced process kinetics. |
| abstractGer |
Abstract Iron disulfide ($ FeS_{2} $) powders were successfully synthesized by hydrothermal method. Cetyltrimethylammonium bromide (CTAB) had a great influence on the morphology, particle size, and electrochemical performance of the $ FeS_{2} $ powders. The as-synthesized $ FeS_{2} $ particles with CTAB had diameters of 2–4 μm and showed a sphere-like structure with sawtooth, while the counterpart prepared without CTAB exhibited irregular morphology with diameters in the range of 0.1–0.4 μm. As anode materials for Li-ion batteries, their electrochemical performances were investigated by galvanostatic charge–discharge test and electrochemical impedance spectrum. The $ FeS_{2} $ powder synthesized with CTAB can sustain 459 and 413 mAh $ g^{−1} $ at 89 and 445 mA $ g^{−1} $ after 35 cycles, respectively, much higher than those prepared without CTAB (411 and 316 mAh $ g^{−1} $). The enhanced rate capability and cycling stability were attributed to the less-hindered surface layer and better electrical contact from the sawtooth-like surface and micro-sized sphere morphology, which led to enhanced process kinetics. |
| abstract_unstemmed |
Abstract Iron disulfide ($ FeS_{2} $) powders were successfully synthesized by hydrothermal method. Cetyltrimethylammonium bromide (CTAB) had a great influence on the morphology, particle size, and electrochemical performance of the $ FeS_{2} $ powders. The as-synthesized $ FeS_{2} $ particles with CTAB had diameters of 2–4 μm and showed a sphere-like structure with sawtooth, while the counterpart prepared without CTAB exhibited irregular morphology with diameters in the range of 0.1–0.4 μm. As anode materials for Li-ion batteries, their electrochemical performances were investigated by galvanostatic charge–discharge test and electrochemical impedance spectrum. The $ FeS_{2} $ powder synthesized with CTAB can sustain 459 and 413 mAh $ g^{−1} $ at 89 and 445 mA $ g^{−1} $ after 35 cycles, respectively, much higher than those prepared without CTAB (411 and 316 mAh $ g^{−1} $). The enhanced rate capability and cycling stability were attributed to the less-hindered surface layer and better electrical contact from the sawtooth-like surface and micro-sized sphere morphology, which led to enhanced process kinetics. |
| collection_details |
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| container_issue |
4 |
| title_short |
Enhanced electrochemical performance of $ FeS_{2} $ synthesized by hydrothermal method for lithium ion batteries |
| url |
https://dx.doi.org/10.1007/s10800-012-0393-5 |
| remote_bool |
true |
| author2 |
Wang, X. L. Mai, Y. J. Xia, X. H. Gu, C. D. Tu, J. P. |
| author2Str |
Wang, X. L. Mai, Y. J. Xia, X. H. Gu, C. D. Tu, J. P. |
| ppnlink |
302466037 |
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| doi_str |
10.1007/s10800-012-0393-5 |
| up_date |
2024-07-03T18:49:31.507Z |
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| score |
7.400736 |